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2000
Volume 20, Issue 2
  • ISSN: 1574-8871
  • E-ISSN: 1876-1038

Abstract

Background

infection is the main cause of most PUD; therefore, the eradication of is extremely important in the treatment of PUD. There are several recommended treatment regimens suggested to eradicate this organism.

Aim

This study compared the efficacy of three anti- regimens in patients with dyspepsia or peptic ulcer disease (PUD).

Objective

The objective of this study was to assess the efficacy of three anti- treatments in patients based on C14 urease breath test (C-UBT) results, drug compliance, and adverse effects.

Methods

This randomized, open-label clinical trial included 136 -infected patients without prior treatment. Patients were randomly divided into three groups. The OAC group received 20 mg Omeprazole capsules twice a day, two 500 mg Amoxicillin capsules twice a day, and 500 mg Clarithromycin capsules twice a day for 14 days. The OAL group received 20 mg Omeprazole capsules twice a day, two 500 mg Amoxicillin capsules twice a day, and Levofloxacin 500 mg capsules twice a day for 14 days. The OAMB group received 20 mg Omeprazole capsules twice a day, two 500 mg Amoxicillin capsules twice a day, Metronidazole 500 mg three times a day, and Bismuth 240 mg twice a day for 14 days. Evaluation for compliance and drug-related adverse effects were assessed at the end of two weeks. eradication was evaluated eight weeks after treatment using the C-UBT.

Results

A total of 136 patients participated in this study, and their groups were matched based on age and sex. The results of the C-UBT test showed that the eradication rate of was 82.2%, 91.3%, and 97.3% for the three-drug OAC, OAMB, and OAL treatment regimens, respectively. Moreover, all the regimens showed high compliance among the patients. Only OAC and OAL showed a significant difference in the eradication rate, and no superiority was found between OAMB and OAL or OAC therapies.

Conclusion

The regime of OAL achieved a satisfactory rate of infection eradication with good tolerance in patients with PUD, without any acute side effects.

Clinical Trial Registration Number

IRCT201605189014N100.

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